Product Name :
2-Amino-4-nitrophenol (CAS 99-57-0)
Synonym :
2-Hydroxy-5-nitroaniline
Application :
CAS:
99-57-0
Purity:
≥95%
Molecular Weight:
154.12
Formula :
C6H6N2O3
Physical state:
Solid
solubility :
Soluble in water (0.9 g/l at 20° C), DMSO, methanol, ether, and ethanol.
Shipping Condition :
Store at room temperature
Melting point:
140-143° C (lit.)
SMILES:
NC1=C(O)C=CC(=C1)[N+]([O-])=O
References:
:Peroxidase-catalyzed co-oxidation of 3,3′,5,5′-tetramethylbenzidine with 2-amino-4-nitrophenol, 4,4′-dihydroxydiphenylsulfone, and their polydisulfides in aqueous and micellar media. | Karasyova, EI., et al. 2001. Biochemistry (Mosc). 66: 608-17. PMID: 11421808Synthesis of Pyrrolo[4,3,2-de]quinolines from 6,7-Dimethoxy-4-methylquinoline. Formal Total Syntheses of Damirones A and B, Batzelline C, Isobatzelline C, Discorhabdin C, and Makaluvamines A-D. | Roberts, D., et al. 1997. J Org Chem. 62: 568-577. PMID: 11671451NTP Toxicology and Carcinogenesis Studies of 2-Amino-4-Nitrophenol (CAS No. 99-57-0) in F344/N Rats and B6C3F1 Mice (Gavage Studies). | ,. 1988. Natl Toxicol Program Tech Rep Ser.2,2-Dimethyl-morpholine structure 339: 1-170.Price of 150852-73-6 PMID: 12724786Continuous biotransformation and removal of nitrophenols under denitrifying conditions. | Karim, K. and Gupta, SK. 2003. Water Res. 37: 2953-9. PMID: 12767298Interactions between nitrate assimilation and 2,4-dinitrophenol cometabolism in Rhodobacter capsulatus E1F1. | Luque-Almagro, VM., et al. 2006. Curr Microbiol. 53: 37-42. PMID: 16775785Synthesis of 2-n-(hexadecanoyl)-amino-4-nitrophenyl phosphorylcholine-hydroxide, a chromogenic substrate for assaying sphingomyelinase activity. | Gal, AE. and Fash, FJ. 1976. Chem Phys Lipids. 16: 71-9. PMID: 177220Final report on the safety assessment of amino nitrophenols as used in hair dyes. | Burnett, CL., et al. 2009. Int J Toxicol. 28: 217S-51S. PMID: 20086194Voltammetric and amperometric determination of 2,4-dinitrophenol metabolites. | Dejmkova, H., et al. 2011. Talanta. 85: 2594-8. PMID: 21962688Syntheses and pH sensing applications of imine-coupled phenol and polyphenol species derived from 2-amino-4-nitrophenol. | Yıldırım, M., et al. 2012. J Fluoresc. 22: 961-70. PMID: 22227702Convergent Synthesis of Dronedarone, an Antiarrhythmic Agent. | Okitsu, T., et al.PMID:33674737 2016. Chem Pharm Bull (Tokyo). 64: 1149-53. PMID: 27477654Does the stability of the stacking motif surpass the planar motif in 2-amino-4-nitrophenol? – a CCSD(T) analysis. | Deepa, P. 2018. J Mol Model. 25: 6. PMID: 30564979Fungicidal Properties of 2-Amino-4-nitrophenol and Its Derivatives. | Mukhtorov, L., et al. 2019. Bull Environ Contam Toxicol. 102: 880-886. PMID: 30923837Plasma levels and kinetic disposition of 2,4-dinitrophenol and its metabolites 2-amino-4-nitrophenol and 4-amino-2-nitrophenol in the mouse. | Robert, TA. and Hagardorn, AN. 1985. J Chromatogr. 344: 177-86. PMID: 4086539Radiochemical synthesis and photochemical properties of the uncoupler 2-azido-4-nitrophenol, a versatile photoaffinity labeling reagent. | Hanstein, WG., et al. 1979. Biochemistry. 18: 1019-25. PMID: 427093Microbial photodegradation of aminoarenes. Metabolism of 2-amino-4-nitrophenol by Rhodobacter capsulatus. | Witte, CP., et al. 1998. Appl Biochem Biotechnol. 69: 191-200. PMID: 9584054